A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218486



Internal ID20785526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99565331..99567188hg38UCSC Ensembl
chr13:100217585..100219442hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg381858
hg191858
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579282
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218486
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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